Clinical heterogeneity of familial spastic paraplegia linked to chromosome 2p21.

Published

Journal Article

The clinical features of four families with autosomal dominant spastic paraparesis (FSP) are described, along with the results of linkage analysis to markers from the regions of chromosomes 2, 14, and 15 which are known to contain spastic paraplegia genes. All families had 'pure' spastic paraparesis (FSP), but the severity of symptoms varied widely among families, and other mild neurologic signs were observed in some subjects. Although no family individually yielded a lod score >3.0, all families yielded positive lod scores with chromosome 2 markers, and a maximal lod score of 5.7 was obtained for the families combined using marker D2S352. There was no evidence of linkage to chromosome 14 or 15 in any of the families.

Full Text

Duke Authors

Cited Authors

  • Nance, MA; Raabe, WA; Midani, H; Kolodny, EH; David, WS; Megna, L; Pericak-Vance, MA; Haines, JL

Published Date

  • May 1998

Published In

Volume / Issue

  • 48 / 3

Start / End Page

  • 169 - 178

PubMed ID

  • 9618065

Pubmed Central ID

  • 9618065

International Standard Serial Number (ISSN)

  • 0001-5652

Digital Object Identifier (DOI)

  • 10.1159/000022798

Language

  • eng

Conference Location

  • Switzerland